WO2002003965A1 - Method for formulating healthcare products with enhanced stability - Google Patents
Method for formulating healthcare products with enhanced stability Download PDFInfo
- Publication number
- WO2002003965A1 WO2002003965A1 PCT/US2001/021418 US0121418W WO0203965A1 WO 2002003965 A1 WO2002003965 A1 WO 2002003965A1 US 0121418 W US0121418 W US 0121418W WO 0203965 A1 WO0203965 A1 WO 0203965A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- active ingredient
- excipients
- polymers
- formulating
- interaction
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/167—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface
- A61K9/1676—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface having a drug-free core with discrete complete coating layer containing drug
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
Definitions
- the present invention relates to improved healthcare product formulations, including solid pharmaceutical dosages.
- This application is related to co-pending application U.S. Serial No. , "Improved Thyroid Hormone Formulations,” filed contemporaneously with the present application and assigned to the same assignee, the disclosure of which is hereby incorporated by reference in its entirety.
- Modern healthcare product manufacturing processes have become increasingly sophisticated. For example, newer techniques for manufacturing pharmaceutical dosages involve higher pressures, dry processing, and the like.
- new compounds are being formulated, including, but not limited to, proteins, peptides, enzymes, hormones, nucleic acids and derivatives thereof (collectively, "drugs of biological origin”). Further, more complex formulations are being manufactured in an attempt not only to improve bioavailability and extend shelf-life, but also to reduce toxicity and to enable site-specific drug delivery.
- Solid pharmaceutical dosages traditionally have included capsules, tablets and other unit dosage forms, each form containing a pharmaceutically or biologically active ingredient and at least one additional "excipient" ingredient.
- the excipient which is intended to be a therapeutically inert and non-toxic carrier, may function, for example, as a diluent, binder, lubricant, disintegrant, stabilizer, buffer or preservative.
- any easily hydrolyzable drug should not be mixed with a hydrated excipient if the water of crystallization could be released by the formulating process.
- the active ingredient has a primary amine function, the use of mono- or di-saccharide excipients may lead to amine-aldehyde and amine-acetal reactions.
- the active ingredient is an ester or lactone, the use of any excipient that might create a basic environment could lead to ester-base hydrolysis.
- Any compound containing an aldehyde moiety should not be mixed with amine type excipients, in order to avoid aldehyde-amine reactions.
- the formation of hydrogen bonds such as those between carbonyl and silanol groups, may destabilize a drug.
- the excipient still may contain some impurities, such as unreacted metals or residual solvents, whose origin lies in the processing of the excipient. These impurities can then react and/or degrade the drug, and reduce its activity.
- impurities such as unreacted metals or residual solvents, whose origin lies in the processing of the excipient.
- ferric iron catalyzes the oxidation of drugs such as hydrocortisone.
- clays containing adsorbed ferric iron should be avoided in formulating drugs prone to such oxidative degradation.
- aldehydes and peroxides may be present as reactive impurities in polyethylene glycol (PEG).
- a method for formulating healthcare products comprising the steps of:
- drugs or pharmaceutical agents can be formulated into a suitable dosage form with increased stability by depositing the pharmaceutical active agent as a pure ingredient onto a substrate in the absence of excipients and then processing into an appropriate dosage form therefrom.
- a pharmaceutical active agent that has been found to have stability problems when admixed with excipients, is deposited, as a dry powder substantially free of excipients, onto the substrate by an electrostatic deposition process. In the electrostatic deposition process, a cloud or stream of charged particles of the active ingredient is exposed to, or directed towards, a substrate, at the surface of which substrate a pattern of opposite charges has been established.
- a measured dosage of the active ingredient can be adhered to a substrate without the need for additional carriers, binders or the like.
- pharmaceutically active agents that normally are unstable when admixed with excipients and/or subjected to normal mechanical processing conditions involved in the manufacture of traditional solid dosage forms, are stable when incorporated into a final dosage form using a process of the invention, involving electrostatic deposition.
- Suitable means of electrostatic deposition are described in, for example, U.S. Patent Nos. 5,714,007, 5,846,595 and 6,074,688, the disclosures of which are incorporated by reference herein in their entireties.
- Active pharmaceutical ingredients that would benefit from the enhanced- stability formulation method of the present invention include, but are not limited to, lansoprazole, molsidomime, topotecan, moexipril, oxprenolol, Astra FLA 336, nifedipine, steroids (e.g., prednisone), nitroglycerine, heparin, and drugs of biological origin. It should be understood that, in addition to the active ingredients included in this list, any other suitable active pharmaceutical ingredient, which demonstrates instability or loss of potency when compressed or when admixed with various excipients, can easily be identified and selected by those of ordinary skill in the art, by routine testing.
- the preferred deposition substrate is a "pharmaceutically acceptable" polymer; that is, one that may be introduced safely into the human or animal body, for example, taken orally and digested. Ideally, the polymer has received regulatory approval and is of GRAS ("Generally Regarded As Safe") status.
- the substrate polymer preferably in the form of a film, may either dissolve or otherwise disintegrate subsequent to introduction into the body, for example, subsequent to or upon ingestion, or the polymer may be substantially inert and pass through the body, provided that the dosage form opens or otherwise releases the pharmaceutical substance from the deposit into the patient's body.
- Suitable materials may include, for example, polymers and copolymers of polyvinyl alcohol, polyvinyl pyrrolidinone, polysaccharide polymers, acrylate polymers, methacrylate polymers, phthalate polymers, polyvinyl acetate, methyl cellulose, carboxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, ethyl cellulose, Eudragits (that is, polymers and copolymers containing methacrylic acid), starch-based polymers, gelatin and the like.
- Preferred dosage forms, as well as additional useful substrate polymers are disclosed in published international patent application number WO 99/63972, the disclosure of which hereby is incorporated by reference herein in its entirety.
- a cover film may be applied to encapsulate the electrostatically deposited active ingredient, and the resulting stable "core" may be further processed into dosage forms resembling conventional tablets, capsules, caplets and the like or processed into non- conventional wafers or stamp-like presentations.
- the preferred dosage forms may be suitable for oral, transdermal or buccal dosing of appropriate drugs.
- the method of the invention provides satisfactorily small dosages as may be required, for example, for insulin and its derivatives, heparin and other orally absorbed drugs.
- the compatibility of various conventional polymer films with levothyroxine sodium was evaluated. The goal was to select a suitable polymer film to maximize the stability of levothyroxine sodium for electrostatic deposition, and to develop a dosage form using selected polymer films.
- Each sample was prepared by depositing levothyroxine sodium on a polymer substrate, in a drug-to-film ratio of approximately 1:14. Samples were stored in individual amber vials with Teflon-lined screw cap closures at 25°C with 60% Relative Humidity and at 40°C with 75% Relative Humidity ("RH"). As a control, levothyroxine sodium drug substance was stored, without any deposition substrate, in closed amber vials under the same conditions as the samples. Samples were analyzed at 4 or 6 weeks for the presence of degradants (and loss of active ingredient) by means of a stability- indicating High Performance Liquid Chromatography method.
- Substrate 1527-79- 1 50% Hydroxypropylmethylcellulose (“HPMC”) + 50% Hydroxypropylcellulose (“HPC”)
- Substrate 1577-7-1 60% Ethyl cellulose ("EC") + 5% HPMC + 35% Triethyl citrate ("TEC") 3.
- Substrate 1577-7-3 60% EC + 5% HPC + 35% TEC
- Substrate 1577-6-3 66% Cellulose acetate phthalate ("CAP") + 5% HPMC + 25% TEC + 4% Polysorbate 80 5.
- Substrate 1527-69-1 45% HPMC + 45% HPC + 10% Polyethylene Glycol 400 ("PEG”) 7.
- Substrate 1527-84-1 100% HPC
- Substrate 1501-56-3 100% HPMC
- the compatibility of three polymer films with ondansetron was evaluated. The goal was to select a suitable polymer film to maximize the stability of ondansetron for electrostatic deposition, and to develop a dosage form using selected polymer films.
- Each sample was prepared by depositing a quantity of ondansetron on a polymer substrate followed by folding of the film.
- Each sample was stored in a high- density polyethylene (HDPE) bottle with polypropylene (PP) screw cap at 25°C with 60% Relative Humidity and at 40°C with 75% Relative Humidity ("RH").
- HDPE high- density polyethylene
- PP polypropylene
- RH Relative Humidity
- ondansetron drug substance was stored, without any substrate, in HDPE bottles with PP screw caps under same conditions as the samples.
- Samples were analyzed at 2 or 4 weeks for the presence of degradants (and loss of active ingredient) by means of a stability- indicating High Performance Liquid Chromatography method.
- Substrate 990210 Purity Gum, Sorbitol and Pectin 2.
- Substrate 990193 45% Hydroxypropylmethylcellulose ("HPMC”) + 45% Hydroxypropylcellulose (“HPC”) + 10% Polyethylene Glycol 400 (“PEG”)
- Substrate 990077 Hydroxypropylmethylcellulose (“HPMC")
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- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002415082A CA2415082A1 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
JP2002508420A JP2004502724A (en) | 2000-07-06 | 2001-07-06 | Formulation of healthcare products with increased stability |
AU2001273231A AU2001273231A1 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
IL15379801A IL153798A0 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
US10/332,255 US20050013924A1 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
EP01952487A EP1296653A4 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
HU0301415A HUP0301415A2 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
KR10-2003-7000124A KR20030023692A (en) | 2000-07-06 | 2001-07-06 | Method for Formulating Healthcare Products with Enhanced Stability |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21620500P | 2000-07-06 | 2000-07-06 | |
US60/216,205 | 2000-07-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002003965A1 true WO2002003965A1 (en) | 2002-01-17 |
Family
ID=22806160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/021418 WO2002003965A1 (en) | 2000-07-06 | 2001-07-06 | Method for formulating healthcare products with enhanced stability |
Country Status (10)
Country | Link |
---|---|
US (1) | US20050013924A1 (en) |
EP (1) | EP1296653A4 (en) |
JP (1) | JP2004502724A (en) |
KR (1) | KR20030023692A (en) |
CN (1) | CN1441669A (en) |
AU (1) | AU2001273231A1 (en) |
CA (1) | CA2415082A1 (en) |
HU (1) | HUP0301415A2 (en) |
IL (1) | IL153798A0 (en) |
WO (1) | WO2002003965A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005015128A1 (en) * | 2005-03-31 | 2006-10-05 | Lts Lohmann Therapie-Systeme Ag | Wafers containing steroid hormones |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7794774B2 (en) * | 2005-11-07 | 2010-09-14 | The Quaker Oats Company | Long shelf-life high moisture content cereal products |
US20090157185A1 (en) * | 2007-12-18 | 2009-06-18 | Chong Chol Kim | Prosthetic Monolithic Spinal Discs and Method of Customizing and Constructing Discs |
US10874615B2 (en) * | 2015-09-14 | 2020-12-29 | Merck Patent Gmbh | Formulation having controlled, delayed release of active ingredient |
MX2022000309A (en) | 2019-07-09 | 2022-03-17 | Oerlikon Metco Us Inc | Iron-based alloys designed for wear and corrosion resistance. |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5714007A (en) * | 1995-06-06 | 1998-02-03 | David Sarnoff Research Center, Inc. | Apparatus for electrostatically depositing a medicament powder upon predefined regions of a substrate |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4031200A (en) * | 1975-12-15 | 1977-06-21 | Hoffmann-La Roche Inc. | Manufacture of pharmaceutical unit dosage forms |
GB2253164B (en) * | 1991-02-22 | 1994-10-05 | Hoechst Uk Ltd | Improvements in or relating to electrostatic coating of substrates of medicinal products |
US5846595A (en) * | 1996-04-09 | 1998-12-08 | Sarnoff Corporation | Method of making pharmaceutical using electrostatic chuck |
KR20010052734A (en) * | 1998-06-10 | 2001-06-25 | 낸시 엠. 그레이 | Pharmaceutical product and methods and apparatus for making same |
-
2001
- 2001-07-06 HU HU0301415A patent/HUP0301415A2/en unknown
- 2001-07-06 US US10/332,255 patent/US20050013924A1/en not_active Abandoned
- 2001-07-06 EP EP01952487A patent/EP1296653A4/en not_active Withdrawn
- 2001-07-06 KR KR10-2003-7000124A patent/KR20030023692A/en not_active Application Discontinuation
- 2001-07-06 WO PCT/US2001/021418 patent/WO2002003965A1/en not_active Application Discontinuation
- 2001-07-06 JP JP2002508420A patent/JP2004502724A/en not_active Withdrawn
- 2001-07-06 AU AU2001273231A patent/AU2001273231A1/en not_active Abandoned
- 2001-07-06 CA CA002415082A patent/CA2415082A1/en not_active Abandoned
- 2001-07-06 CN CN01812403A patent/CN1441669A/en active Pending
- 2001-07-06 IL IL15379801A patent/IL153798A0/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5714007A (en) * | 1995-06-06 | 1998-02-03 | David Sarnoff Research Center, Inc. | Apparatus for electrostatically depositing a medicament powder upon predefined regions of a substrate |
US6074688A (en) * | 1995-06-06 | 2000-06-13 | Delsys Pharmaceautical Corporation | Method for electrostatically depositing a medicament powder upon predefined regions of a substrate |
Non-Patent Citations (1)
Title |
---|
See also references of EP1296653A4 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005015128A1 (en) * | 2005-03-31 | 2006-10-05 | Lts Lohmann Therapie-Systeme Ag | Wafers containing steroid hormones |
DE102005015128B4 (en) * | 2005-03-31 | 2008-12-11 | Bayer Schering Pharma Aktiengesellschaft | Wafers containing steroid hormones |
US9763960B2 (en) | 2005-03-31 | 2017-09-19 | Lts Lohmann Theraple-Systeme Ag | Wafer comprising steroid hormones |
Also Published As
Publication number | Publication date |
---|---|
EP1296653A4 (en) | 2005-09-21 |
CA2415082A1 (en) | 2002-01-17 |
US20050013924A1 (en) | 2005-01-20 |
KR20030023692A (en) | 2003-03-19 |
JP2004502724A (en) | 2004-01-29 |
EP1296653A1 (en) | 2003-04-02 |
HUP0301415A2 (en) | 2003-09-29 |
CN1441669A (en) | 2003-09-10 |
AU2001273231A1 (en) | 2002-01-21 |
IL153798A0 (en) | 2003-07-31 |
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